eudamed_udi
Primary ID: 05059441141570
Ninjo (UDI 05059441141570)
Manufactured by ArjoHuntleigh AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ninjo - Primary ID 05059441141570
Device Regulatory Overview
The Ninjo (Model/Catalog Number: FA0A012KACZ0) is a medical device manufactured by ArjoHuntleigh AB. This product is indexed under FDA Product Code / Category Classification Z12011301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FA0A012KACZ0
- Product Code / EMDN
- Z12011301
- Device Name
- NINJO
- Database Sync Date
- 2026-08-09 16:28:57
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Ninjo?
The registered manufacturer of record for Ninjo is ArjoHuntleigh AB.
What is the Primary UDI-DI identifier for Ninjo?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05059441141570.
What classification code is assigned to this device?
This device is registered under product classification code Z12011301.
Similar Classification Devices (Z12011301)
Other Devices by ArjoHuntleigh AB
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint